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825613-16-9

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825613-16-9 Usage

Type of compound

Benzimidazole derivative

Pharmacological activities

Diverse range

Potential use

Building block in the synthesis of biologically active molecules

Functional groups

Benzimidazole and dicarbonitrile

Applications

Medicinal chemistry and pharmaceutical research

Potential role

Precursor in the development of new drugs targeting specific biological pathways

Structural feature

Inclusion of a phenyl group

Check Digit Verification of cas no

The CAS Registry Mumber 825613-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,5,6,1 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 825613-16:
(8*8)+(7*2)+(6*5)+(5*6)+(4*1)+(3*3)+(2*1)+(1*6)=159
159 % 10 = 9
So 825613-16-9 is a valid CAS Registry Number.

825613-16-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1H-benzimidazole-5,6-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 2-phenylbenzimidazole-5,6-dicarbonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:825613-16-9 SDS

825613-16-9Relevant articles and documents

FLUORESCENCE LABELING AGENT, PHOTODYNAMIC THERAPEUTIC AGENT AND PHTHALOCYANINE

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Paragraph 0068; 0070, (2021/04/23)

PROBLEM TO BE SOLVED: To provide a phthalocyanine-based compound having excellent properties such as fluorescence intensity, light resistance and singlet oxygen generation ability suitable for a fluorescence labeling agent and a photodynamic therapeutic agent in a wavelength region of 800 nm or more. SOLUTION: This invention relates to salts of a phosphorus-containing phthalocyanine-based compound in which a phosphorus atom in a phosphorus compound expressed by formula: R5O-P-OR6 is coordinated with a phthalocyanine-based compound, and to a fluorescence labeling agent and a photodynamic therapeutic agent, which contain the salts of the phosphorus-containing phthalocyanine-based compound. In the formula, R5 and R6 are H, an aliphatic hydrocarbon group, -P(=O) R7R8, -C(=O) R9, -S(=O)2R10 or -SiR11R12R13; R7 and R8 are H, OH, an aliphatic hydrocarbon group, an aromatic hydrocarbon group, an alkoxyl group, or an aryloxy group; R9 is H, an aliphatic hydrocarbon group, or an aromatic hydrocarbon group; R10 is OH, an aliphatic hydrocarbon group, or an aromatic hydrocarbon group; and R11 to R13 are an aliphatic hydrocarbon group or an aromatic hydrocarbon group. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Substituted benzazoloporphyrazines for polymerization and surface attachment and articles formed therefrom

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Page/Page column 27, (2011/02/18)

The present invention provides an article of manufacture formed from a substrate and a benzazoloporphyrazine bound to the substrate. The article may take a variety of different forms and may be for example an electrochromic display, a molecular capacitor, a battery, a solar cell, or a molecular memory device. Methods of making such articles, along with compounds, methods and intermediates useful for making such benzazoloporphyrazines, are also described.

Metal complexes of phthalocyanine structural analogs with oxygen- or nitrogen-containing heterorings. Synthesis and properties

Maizlish,Shaposhnikov,Balakireva,Zharnikova,Abramov,Ivanovskii,Smirnov

, p. 787 - 790 (2007/10/03)

Nucleophilic substitution of the bromine atom and nitro group in 4-bromo-5-nitrophthalodinitrile and reduction of 4-benzoylamino-5- nitrophthalodinitrile gave, respectively, tribenzo[b,e,g][1,4]dioxocine-7,8- dicarbonitrile and 2-phenylbenzimidazole-5,6-d

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